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filingDate 1994-07-12^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1995-08-15^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2b20fe04450c387270aa9c57e5b81950
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f2f5a9398606ec2ef27fa1bc111ea9f9
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3746d30f79737c5abcbcf7941cc9ce22
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e1296102fef4c23ea72709454ac6259a
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d38a4b3478c5c5e92c329d85dd90a4a1
publicationDate 1995-08-15^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-5441975-A
titleOfInvention Pyrazolo-substituted alkyl amide acat inhibitors
abstract Pharmaceutically useful compounds having ACAT inhibitory activity of the formula <IMAGE> wherein n is 0, 1, or 2, for X other than tetrazole and n=2 then R2=R3=H; R1 is phenyl, substituted phenyl, naphthyl, substituted naphthyl, a heteroaromatic group or a hydrocarbon group having from one to 18 carbon atoms; R2 and R3 are hydrogen, halo, hydroxy, alkyl, alkenyl, cycloalkyl, phenyl, substituted phenyl, a heteroaryl, or form a spiroalkyl group; X is a heteromonocyclic 5-membered ring containing one to four heteroatoms, said heteroatoms being nitrogen, oxygen or sulfur, and combination thereof; and R4 is a hydrocarbon group having from one to 20 carbon atoms are described as well as methods of their manufacture.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2005234124-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-8466165-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2010190977-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2005250761-A1
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http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-8623883-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5861398-A
priorityDate 1991-08-22^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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